Tissue Eng Regen Med.  2017 Aug;14(4):443-452. 10.1007/s13770-017-0048-z.

Heparin/Collagen 3D Scaffold Accelerates Hepatocyte Differentiation of Wharton's Jelly-Derived Mesenchymal Stem Cells

Affiliations
  • 1Department of Biology, Kharazmi University, No. 43, South Mofatteh Ave, Tehran 15712-14911, Iran.
  • 2Biochemistry Department, Shiraz University of Medical Sciences, Mehr Intersection, Qasr-Dasht st., District 1, Shiraz, Fars 71345, Iran.
  • 3Tissue Engineering Lab, Anatomy Department, Shiraz Medical School, Shiraz University of Medical Sciences, Mehr Intersection, Qasr-Dasht st., District 1, Shiraz, Fars 71345, Iran. talaeit@sums.ac.ir
  • 4Institute for Cancer Research, Shiraz University of Medical Sciences, Mehr Intersection, Qasr-Dasht st., District 1, Shiraz, Fars 71345, Iran.

Abstract

Both mature and stem cell-derived hepatocytes lost their phenotype and functionality under conventional culture conditions. However, the 3D scaffolds containing the main extracellular matrix constitutions, such as heparin, may provide appropriate microenvironment for hepatocytes to be functional. The current study aimed to investigate the efficacy of the differentiation capability of hepatocytes derived from human Wharton's jelly mesenchymal stem cells (WJ-MSCs) in 3D heparinized scaffold. In this case, the human WJ-MSCs were cultured on the heparinized and non-heparinized 2D collagen gels or within 3D scaffolds in the presence of hepatogenic medium. Immunostaining was performed for anti-alpha fetoprotein, cytokeratin-18 and -19 antibodies. RT-PCR was performed for detection of hepatic nuclear factor-4 (HNF-4), albumin, cytokeratin-18 and -19, glucose-6-phosphatase (G6P), c-met and Cyp2B. The results indicated that hepatogenic media induced the cells to express early liver-specific markers including HNF4, albumin, cytokeratin-18 and 19 in all conditions. The cells cultured on both heparinized culture conditions expressed late liver-specific markers such as G6P and Cyp2B as well. Besides, the hepatocytes differentiated in 3D heparinized scaffolds stored more glycogen that indicated they were more functional. Non-heparinized 2D gel was the superior condition for cholangiocyte differentiation as indicated by higher levels of cytokeratin 19 expression. In conclusion, the heparinized 3D scaffolds provided a microenvironment to mimic Disse space. Therefore, 3D heparinized collagen scaffold can be suggested as a good vehicle for hepatocyte differentiation.

Keyword

Hepatocytes; Collagen type I; Heparin; Scaffold; Gel

MeSH Terms

Antibodies
Collagen
Collagen Type I
Constitution and Bylaws
Extracellular Matrix
Fetal Proteins
Gels
Glucose-6-Phosphatase
Glycogen
Heparin
Hepatocytes*
Humans
Keratin-18
Keratin-19
Mesenchymal Stromal Cells*
Phenotype
Wharton Jelly
Antibodies
Collagen
Collagen Type I
Fetal Proteins
Gels
Glucose-6-Phosphatase
Glycogen
Heparin
Keratin-18
Keratin-19
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